Xie W Q, Potts M
Department of Biochemistry, Virginia Polytechnic Institute and State University, Blacksburg 24060.
Arch Biochem Biophys. 1991 Jan;284(1):22-5. doi: 10.1016/0003-9861(91)90256-i.
The core enzyme of the cyanobacterial DNA-dependent RNA polymerase contains a unique component, gamma, which is absent from the corresponding enzymes of other eubacteria. In the heterocystous cyanobacterium Nostoc commune the gene encoding gamma, rpoC1, is immediately adjacent to, and downstream of, rpoB. The rpoC1 gene, and a 3' adjacent gene, rpoC2, correspond to the single rpoC gene found in Escherichia coli with respect to those domains conserved within their translational products. Northern analysis and primer extension assay show that in N. commune, rpoC1 and rpoC2 are transcribed separately from rpoB. The promoter of rpoC1C2 can direct the expression of a promotorless lacZ gene in E. coli. As a consequence, cyanobacterial rpo gene expression is distinct from the mode of cotranscription described for the equivalent sequences found in other eubacteria, archaebacteria, and plant chloroplasts. Also in this paper, a simple protocol for RNA isolation, which should be applicable for RNA isolation from plant cells, is presented.
蓝藻DNA依赖的RNA聚合酶的核心酶含有一个独特的组分γ,而其他真细菌的相应酶中没有该组分。在异形胞蓝藻集胞藻中,编码γ的基因rpoC1紧邻rpoB且位于其下游。就其翻译产物中保守的那些结构域而言,rpoC1基因以及一个3' 相邻基因rpoC2与大肠杆菌中发现的单个rpoC基因相对应。Northern分析和引物延伸试验表明,在集胞藻中,rpoC1和rpoC2与rpoB是分开转录的。rpoC1C2的启动子能够指导无启动子的lacZ基因在大肠杆菌中的表达。因此,蓝藻rpo基因的表达不同于在其他真细菌、古细菌和植物叶绿体中发现的等效序列所描述的共转录模式。本文还给出了一个简单的RNA分离方案,该方案应该适用于从植物细胞中分离RNA。